Lilly’s Neutralizing Antibody Bamlanivimab (LY-CoV555) Receives FDA Emergency Use Authorization for the Treatment of Recently Diagnosed COVID-19
The Pharma Data
NOVEMBER 9, 2020
Bamlanivimab remains an investigational drug and has not been approved under a Biologics License Application (BLA). Lilly is in discussions with global regulators to make bamlanivimab available around the world. The authorization is temporary and does not replace the formal review and approval process.
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